P190-B是一种rho - gtpase激活蛋白,在终末芽和乳腺癌中存在差异表达。

G Chakravarty, D Roy, M Gonzales, J Gay, A Contreras, J M Rosen
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引用次数: 0

摘要

采用显微解剖和差异显示PCR技术,对45日龄初生大鼠乳腺高增殖终末芽(TEBs)中优先表达的基因进行鉴定。其中一个克隆与人类编码新型Rho-Gap的p190-B基因具有87%的同源性。原位杂交发现,p190-B在teb和末端导管中均有表达,在teb的外层表达量最高。在正常乳腺发育过程中,p190-B mRNA在初生乳腺中表达最高,在妊娠晚期和哺乳期表达降低。有趣的是,与正常乳腺相比,p190-B mRNA水平升高出现在小鼠乳腺肿瘤的一个亚群中,这些肿瘤分化程度较低,可能更具侵袭性。将p190-B表达构建体短暂转染到MCF-10A人乳腺上皮细胞中,可导致肌动蛋白细胞骨架的破坏,这表明p190-B在调节影响细胞迁移和侵袭的信号通路中发挥作用。这些结果表明,p190-B可能是乳腺发育所必需的,其异常表达可能发生在乳腺癌中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
P190-B, a Rho-GTPase-activating protein, is differentially expressed in terminal end buds and breast cancer.

Microdissection and differential display PCR were used to identify genes preferentially expressed in the highly proliferative terminal end buds (TEBs) in the mammary gland of 45-day-old virgin rats. One clone exhibited 87% homology to the human p190-B gene encoding a novel Rho-Gap. Using in situ hybridization, p190-B was detected in both the TEBs and the terminal ducts, with the highest expression observed in the outer layer of TEBs. During normal mammary gland development, p190-B mRNA expression was highest in the virgin mammary gland and decreased during late pregnancy and lactation. Interestingly, increased levels of p190-B mRNA relative to the normal mammary gland were seen in a subset of murine mammary tumors that appeared to be less well differentiated and potentially more aggressive. Transient transfection of a p190-B expression construct into MCF-10A human mammary epithelial cells resulted in disruption of the actin cytoskeleton, which suggests a role for p190-B in regulating the signaling pathways that influence cell migration and invasion. These results suggest that p190-B may be required for virgin mammary gland development, and its aberrant expression may occur in breast cancer.

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